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Orthodyne, Inc.
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ISKD (INTRAMEDULLARY SKELETAL KINETIC DISTRACTOR) is an FDA 510(k)-cleared medical device (K010322) manufactured by Orthodyne, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 1, 2001. Regulation: 8.